宁波泰斯拓生物

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SVR (SVEN 1 ras)

货号 TS210842
中文名称 null
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产品名称: SVR (SVEN 1 ras)
商品货号: TS210842
Organism: Mus musculus, mouse
Tissue: pancreas; islet of Langerhans; endothelium
Cell Type: SV40 transformed
Product Format: frozen
Culture Properties: adherent
Biosafety Level: 2 Cells contain polyomavirus DNA sequences

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Strain: C57BL/6
Applications:
The tumors in nude mice cause death by hemorrhage and anemia with thrombocytopenia, and can be used to test angiogenesis inhibitors.
Storage Conditions: liquid nitorgen vapor phase
Derivation:
SVR is a derivative of MS1, a pancreatic islet endothelial cell line (see ATCC CRL-2279).
Receptor Expression:
vascular endothelial growth factor (VEGF)
Genes Expressed:
tissue inhibitor of bioreactive matrix metalloproteinase (high levels)
Cellular Products:
tissue inhibitor of bioreactive matrix metalloproteinase (high levels)
Tumorigenic: Yes
Effects:
Yes, forms aggressive angiosarcomas in nude mice
Comments:
SVR is a derivative of MS1, a pancreatic islet endothelial cell line (see ATCC CRL-2279).
MS1 cells were transduced with a retrovirus encoding H-ras and hygromycin resistance.
The tumors in nude mice cause death by hemorrhage and anemia with thrombocytopenia, and can be used to test angiogenesis inhibitors.
Complete Growth Medium: The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 5%.
Subculturing: Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.53mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: 1:4 to 1:8
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a Manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994.

Cryopreservation:

Complete growth medium described above supplemented with 5% (v/v) DMSO.xa0 Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions:
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
Name of Depositor: JL Arbiser
Deposited As: Mus musculus
References:

Arbiser JL, et al. Oncogenic H-ras stimulates tumor angiogenesis by two distinct pathways. Proc. Natl. Acad. Sci. USA 94: 861-866, 1997. PubMed: 9023347

Tsou R, et al. Retroviral delivery of dominant-negative vascular endothelial growth factor receptor type 2 to murine wounds inhibits wound angiogenesis. Wound Repair Regen. 10: 222-229, 2002. PubMed: 12191004

Hay, R. J., Caputo, J. L., and Macy, M. L., Eds. (1992), ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.

Caputo, J. L., Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988.

Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC.

Biosafety in Microbiological and Biomedical Laboratories, 5th ed. HHS. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Washington DC: U.S. Government Printing Office; 2007. The entire text is available online.